Butylamine → HCID 178449181, compound
Reaction equation
[CH2:1]([NH2:5])[CH2:2][CH2:3][CH3:4].[CH:6]([N:9]=[C:10]=[N:11][CH:12]([CH3:14])[CH3:13])([CH3:8])[CH3:7]>>[CH2:1]([NH:5][C:10]([NH:11][CH:12]([CH3:14])[CH3:13])=[N:9][CH:6]([CH3:8])[CH3:7])[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
A mixture of 33 g of N-butylamine (0.45 mol) and 19 g of diisopropylcarbodiimide (0.15 mol) is refluxed for 3 h 30. GC analysis then shows a conversion of greater than 99.5% of the diisopropylcarbodiimide. The colorless final mixture is concentrated at 60° C. under 20 mbar for 2 h so as to give 29 g of a colorless and virtually odorless liquid of low viscosity, corresponding to the expected guanidine (yield 96.7%).
Workup
- temperatureis refluxed for 3 h 30
- concentrationThe colorless final mixture is concentrated at 60° C. under 20 mbar for 2 h so as
- customto give 29 g of a colorless and virtually odorless liquid of low viscosity
Sources & evidence
- ORD record
- ord-4e97fe162807494a81c988c166351140
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08420761B2
Reaction notes
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